"Ambry Genetics"[submitter] AND "SERPINB9"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2521629	NM_004155.6(SERPINB9):c.1081C>T (p.His361Tyr)	SERPINB9, SERPINB9-AS1 (H361Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295331	NM_004155.6(SERPINB9):c.1079G>A (p.Arg360Lys)	SERPINB9, SERPINB9-AS1 (R360K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525042	NM_004155.6(SERPINB9):c.1039C>T (p.Pro347Ser)	SERPINB9, SERPINB9-AS1 (P347S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160462	NM_004155.6(SERPINB9):c.998C>T (p.Ser333Leu)	SERPINB9, SERPINB9-AS1 (S333L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398394	NM_004155.6(SERPINB9):c.985G>A (p.Ala329Thr)	SERPINB9, SERPINB9-AS1 (A329T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480737	NM_004155.6(SERPINB9):c.965T>C (p.Val322Ala)	SERPINB9, SERPINB9-AS1 (V322A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160461	NM_004155.6(SERPINB9):c.914C>T (p.Ala305Val)	SERPINB9, SERPINB9-AS1 (A305V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317247	NM_004155.6(SERPINB9):c.902C>T (p.Ser301Leu)	SERPINB9, SERPINB9-AS1 (S301L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160460	NM_004155.6(SERPINB9):c.889A>G (p.Lys297Glu)	SERPINB9, SERPINB9-AS1 (K297E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160458	NM_004155.6(SERPINB9):c.794T>C (p.Val265Ala)	SERPINB9, SERPINB9-AS1 (V265A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363889	NM_004155.6(SERPINB9):c.758C>T (p.Ala253Val)	SERPINB9, SERPINB9-AS1 (A253V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601548	NM_004155.6(SERPINB9):c.740C>G (p.Thr247Ser)	SERPINB9, SERPINB9-AS1 (T247S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160457	NM_004155.6(SERPINB9):c.669G>T (p.Arg223Ser)	SERPINB9, SERPINB9-AS1 (R223S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481452	NM_004155.6(SERPINB9):c.637C>T (p.Arg213Cys)	SERPINB9, SERPINB9-AS1 (R213C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291199	NM_004155.6(SERPINB9):c.550C>T (p.Pro184Ser)	SERPINB9, SERPINB9-AS1 (P184S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160456	NM_004155.6(SERPINB9):c.510G>C (p.Lys170Asn)	SERPINB9, SERPINB9-AS1 (K170N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377563	NM_004155.6(SERPINB9):c.469A>G (p.Thr157Ala)	SERPINB9, SERPINB9-AS1 (T157A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367464	NM_004155.6(SERPINB9):c.458T>C (p.Ile153Thr)	SERPINB9, SERPINB9-AS1 (I153T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205235	NM_004155.6(SERPINB9):c.458T>A (p.Ile153Asn)	SERPINB9, SERPINB9-AS1 (I153N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537334	NM_004155.6(SERPINB9):c.446C>T (p.Pro149Leu)	SERPINB9, SERPINB9-AS1 (P149L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317616	NM_004155.6(SERPINB9):c.413A>G (p.Lys138Arg)	SERPINB9, SERPINB9-AS1 (K138R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345280	NM_004155.6(SERPINB9):c.373G>T (p.Ala125Ser)	SERPINB9, SERPINB9-AS1 (A125S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519297	NM_004155.6(SERPINB9):c.335A>G (p.Tyr112Cys)	SERPINB9, SERPINB9-AS1 (Y112C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375393	NM_004155.6(SERPINB9):c.308C>T (p.Thr103Met)	SERPINB9, SERPINB9-AS1 (T103M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265369	NM_004155.6(SERPINB9):c.281G>T (p.Gly94Val)	SERPINB9, SERPINB9-AS1 (G94V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364481	NM_004155.6(SERPINB9):c.274C>T (p.Leu92Phe)	SERPINB9, SERPINB9-AS1 (L92F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356026	NM_004155.6(SERPINB9):c.263C>T (p.Thr88Met)	SERPINB9, SERPINB9-AS1 (T88M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241164	NM_004155.6(SERPINB9):c.230T>C (p.Val77Ala)	SERPINB9, SERPINB9-AS1 (V77A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620736	NM_004155.6(SERPINB9):c.215C>T (p.Ser72Leu)	SERPINB9, SERPINB9-AS1 (S72L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3160454	NM_004155.6(SERPINB9):c.162G>A (p.Met54Ile)	SERPINB9, SERPINB9-AS1 (M54I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160453	NM_004155.6(SERPINB9):c.104T>A (p.Ile35Asn)	SERPINB9, SERPINB9-AS1 (I35N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2294487	NM_004155.6(SERPINB9):c.73T>G (p.Ser25Ala)	SERPINB9, SERPINB9-AS1 (S25A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2258480	NM_004155.6(SERPINB9):c.40C>T (p.Arg14Cys)	SERPINB9, SERPINB9-AS1 (R14C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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Items: 33